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Unrated Drug recall · FDA · Published February 25, 2016

Torrent Recalls Telmisartan 80mg Tablets Due to Silicone Contamination

Torrent Pharma recalls 20,952 cartons of Telmisartan 80mg tablets due to foreign silicone matter. Check your lot BBV8B002R.

🇺🇸 FDA recall #D-0824-2016DrugTorrent Pharma ›
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Recalling firmTorrent Pharmaceuticals LimitedAhmedabad Mehsana Highway · Kadi, India
✎ GovInfoNow plain-language explainer

What happened, in plain English

Torrent Pharmaceuticals Limited is recalling one lot of Telmisartan Tablets, USP, 80 mg because complaints identified the presence of a foreign substance, specifically silicone, within the tablet. The recall affects 20,952 cartons distributed nationwide. The record does not specify any reported injuries or provide a remedy for consumers. Read more at govinfonow.com/recall/43136-torrent-recalls-telmisartan-80mg-tablets-due-to-silicone-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/43136-torrent-recalls-telmisartan-80mg-tablets-due-to-silicone-contamination · Updated October 11, 2026 · FDA enforcement record: FDA #D-0824-2016

Cite this page

“Torrent Recalls Telmisartan 80mg Tablets Due to Silicone Contamination.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43136-torrent-recalls-telmisartan-80mg-tablets-due-to-silicone-contamination. Based on FDA recall #D-0824-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0824-2016%22&limit=1).

Why it’s dangerous

The hazard is the presence of a foreign substance identified as silicone within the tablet itself. The record does not describe the specific health risks or injury mechanisms associated with ingesting this contaminant.

Who’s affected

Patients prescribed Telmisartan 80 mg tablets who purchased the affected product between its manufacture and the recall date. Individuals with this specific prescription are at risk of ingesting foreign material.

How to tell if you have this one

Look for Telmisartan Tablets, USP, 80 mg, in a 30-count carton containing 3 x 10 unit-dose blisters. Check for NDC 13668-158-72, UPC 3 13668 158 72 4, and Lot number BBV8B002R with an expiration date of 12/16.

  • Brand
    Torrent Pharma
  • Product
    Telmisartan Tablets, USP, 80 mg, 30-count (3 x 10 unit-dose blisters) per carton, Rx only, Manufactured by: Torrent
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Feb 25, 201612. FDA classified it Class III: Apr 18, 201623. Published in FDA’s Enforcement Report: Apr 27, 201634. FDA terminated the recall: Jun 3, 201642016
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0824-2016 (February 25, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0824-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA